CN108547152B - Preparation method of washing-resistant, moisturizing, easy-decontamination and soft cotton textiles - Google Patents

Preparation method of washing-resistant, moisturizing, easy-decontamination and soft cotton textiles Download PDF

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CN108547152B
CN108547152B CN201810396357.4A CN201810396357A CN108547152B CN 108547152 B CN108547152 B CN 108547152B CN 201810396357 A CN201810396357 A CN 201810396357A CN 108547152 B CN108547152 B CN 108547152B
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dihydric alcohol
soft
chain
isocyanate
washing
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CN108547152A (en
Inventor
闵洁
顾永星
张战旗
曹春祥
华里发
黄张秘
齐元璋
许秋生
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Shanghai Runying New Material Technology Co ltd
Shanghai Textile Research Institute Co ltd
Shanghai Three Gun Group Co ltd
Donghua University
Lufeng Weaving and Dyeing Co Ltd
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Shanghai Runying New Material Technology Co ltd
Shanghai Textile Research Institute Co ltd
Shanghai Three Gun Group Co ltd
Donghua University
Lufeng Weaving and Dyeing Co Ltd
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
    • D06M15/647Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing polyether sequences
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30Low-molecular-weight compounds
    • C08G18/32Polyhydroxy compounds; Polyamines; Hydroxyamines
    • C08G18/3203Polyhydroxy compounds
    • C08G18/3206Polyhydroxy compounds aliphatic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30Low-molecular-weight compounds
    • C08G18/32Polyhydroxy compounds; Polyamines; Hydroxyamines
    • C08G18/3203Polyhydroxy compounds
    • C08G18/3215Polyhydroxy compounds containing aromatic groups or benzoquinone groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4833Polyethers containing oxyethylene units
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/60Polyamides or polyester-amides
    • C08G18/603Polyamides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6666Compounds of group C08G18/48 or C08G18/52
    • C08G18/667Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/6674Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/564Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
    • D06M15/568Reaction products of isocyanates with polyethers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/02Natural fibres, other than mineral fibres
    • D06M2101/04Vegetal fibres
    • D06M2101/06Vegetal fibres cellulosic
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/01Stain or soil resistance
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/50Modified hand or grip properties; Softening compositions

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

本发明公开了一种耐洗涤保湿易去污柔软性全棉纺织品的制备方法,其特征在于,采用两种整理剂整理全棉纺织品,其中一种为水性改性聚氨酯结构,其包含聚谷氨酸链段和聚醚链段,且含有可反应的封端异氰酸酯结构;另一种为水性聚醚改性胺基有机硅结构,其除含有嵌段连结的胺基硅氧烷链和聚醚链结构。本发明获得的纺织品具有安全环保、效果优异,可用着内衣面料、床用面料,具有柔软、保湿和易洗涤的功能;该功能整理工艺简单易行,过程易于控制,便于大规模生产。The invention discloses a preparation method of a cotton textile that is durable, moisturizing, easy to decontaminate and soft. Acid segment and polyether segment, and contain reactive blocked isocyanate structure; the other is water-based polyether-modified aminosilicon structure, which contains block-linked aminosiloxane chain and polyether chain structure. The textiles obtained by the invention are safe and environmentally friendly, have excellent effects, can be used as underwear fabrics and bedding fabrics, and have the functions of softness, moisture retention and easy washing; the functional finishing process is simple and easy to implement, the process is easy to control, and it is convenient for mass production.

Description

Preparation method of washing-resistant, moisturizing and soil-release soft all-cotton textile
Technical Field
The invention relates to a preparation method of a multifunctional textile, in particular to a washing-resistant, moisturizing and soil-release soft all-cotton textile and a preparation method thereof, and belongs to the technical field of chemical finishing and processing of textiles.
Background
The skin is the natural coat of the human body and is generally divided into three major parts, namely epidermis, dermis and subcutaneous tissue from outside to inside, and the stratum corneum which is the outermost layer of the skin plays an important role in the integrity of the barrier function of the skin. The cuticle has a sebum membrane which is a semitransparent oily membrane formed by sebum, sweat and epidermal cell secretion, free fatty acid, lactate, urea and uric acid in the sebum membrane are natural moisturizing factors and play a role in moisturizing the skin, the cuticle and the sebum membrane can prevent the moisture loss of the skin, and under the normal condition, the water content of the cuticle is about 10 percent and is lower than the level, the surface water shortage symptom can be generated.
The dry skin refers to the condition that the skin becomes thick and rough due to the reasons of water shortage and the like caused by seasonal changes; in autumn and winter, sebum and moisture secretion of human bodies are gradually reduced, the skin becomes dry obviously, particularly, the skin surface of middle-aged and old people is thicker and drier due to the great reduction of moisture, the phenomena of chapping and pruritus at hands, feet and shanks can be caused, and the phenomena of inflammation or purulence and the like caused by chapping of the skin can be caused in serious cases.
The pure cotton fabric is a natural fiber which is deeply favored by consumers, can absorb moisture into the surrounding atmosphere, has the standard moisture content of about 8 percent, and has the moisture content far lower than the requirement of normal skin of a human body on the environmental humidity in winter, so that the pure cotton fabric is easy to cause skin itch of middle-aged and elderly people and other physiological symptoms which influence the body health.
The performance of all-cotton textiles, especially underwear, as the second layer of skin of human body is closely related to the comfort and health of human body to a great extent, and the development of textiles with health care function is a new requirement of the current textile market and people for high-quality life.
Softeners are a class of chemicals that change the static and dynamic coefficients of friction of the fibers. When the dynamic and static friction coefficients of the fiber surface are changed, the resistance which needs to be overcome when the fibers and the skin move mutually can be changed, and the soft and smooth tactile effect is realized, and the tactile effect is a quality index which can be evaluated by a consumer in charge and has important influence on the sale of commodities. Soft finishing is an important after-finishing process in printing and dyeing processing. During the processing of the textile, the hand feeling of the textile becomes rough after being treated for many times, and the common synthetic fiber fabrics are worse, especially the superfine fiber fabrics. In order to make the fabric have soft, smooth and comfortable hand feeling, the fabric needs to be finished, and the finishing is widely performed by using a softening agent at present.
The product has the advantages of developing the functions of moisturizing, easy decontamination, softness and washing resistance of the all-cotton fabric, aiming at enriching the function finishing category of the cotton fabric and improving the clothing quality of the cotton fabric, and has wide development and application prospects from the current health care perspective.
Disclosure of Invention
The invention aims to solve the problems that: the all-cotton textile has good water absorption, and is easy to cause the problems of dry skin, pruritus and the like when worn next to the skin.
In order to solve the problems, the invention provides a preparation method of a washing-resistant, moisturizing and soil-release soft all-cotton textile, which is characterized in that the all-cotton textile is finished by two finishing agents, wherein one finishing agent is aqueous modified polyurethane which comprises a polyglutamic acid chain segment and a polyether chain segment and contains reactive blocked isocyanate; the other is water-based polyether modified amino organic silicon which contains segmented amino siloxane chain links and polyether chain link structures.
Preferably, the number average molecular weight of the polyglutamic acid chain segment is not less than 1000, and the weight percentage of the molecular chain segment in the waterborne modified polyurethane structure is more than 25 percent, so as to meet the requirement of the fiber on the moisture retention performance; the weight percentage of the polyether chain segment in the waterborne modified polyurethane structure is more than 50 percent so as to meet the easy decontamination of the fiber in the washing process.
Preferably, the water-based polyether modified amino organic silicon structure has the functions of softness and smoothness, the amino organic silicon is a polymethyl siloxane macromolecular chain, and a side group of the polymethyl siloxane macromolecular chain contains aminopropyl, N- (beta-aminoethyl) -gamma-aminopropyl or gamma- (2, 3-epoxypropoxy) propyl reactive groups, and the reactive groups can perform a crosslinking reaction with a latent active agent in the modified polyurethane structure in the post-finishing process, so that the washing resistance of functional indexes on cotton fabrics is realized; the polyether chain structure is a polyepoxy ethyl ether structure or a block ether structure of epoxy ethylene and epoxy propylene.
Preferably, the preparation method of the waterborne modified polyurethane structure finishing agent comprises the following steps:
step 1): reacting isocyanate tripolymer and dehydrated high-molecular dihydric alcohol in a reaction kettle at 50-95 ℃ for 2-6 h under the action of a catalyst;
step 2): adding micromolecular dihydric alcohol into a reaction kettle to perform chain extension reaction for 2-3 h, and then adding an end capping agent to continue the reaction for 2-3 h;
step 3): cooling the reaction kettle to 50-60 ℃, adding a polyglutamic acid aqueous solution with the pH value of 4-5, and carrying out chain extension reaction for 4-6 h;
step 4): the reaction kettle is cooled to 25 ℃, and the pH value is adjusted to be neutral by sodium hydroxide.
More preferably, the isocyanate trimer in the step 1) adopts an aliphatic isocyanate trimer or an aromatic toluene diisocyanate trimer; the dehydrated macromolecule dihydric alcohol adopts polyoxyethylene ether dihydric alcohol, block dihydric alcohol of polyoxyethylene polyoxypropylene ether or mixture of two types of dihydric alcohol; the number average molecular weight of the dehydrated macromolecule dihydric alcohol is 500-15000; the molar ratio of the isocyanate tripolymer to the dehydrated high-molecular diol is 2.1-2.4: 1.
More preferably, the small molecule diol in the step 2) adopts ethylene glycol, propylene glycol, butanediol or 1, 4-dimethylol benzene; the end-capping reagent adopts oxime compounds; the molar ratio of the dehydrated polyoxyethylene ether to the micromolecular dihydric alcohol is 4.1-4.2: 1; the molar ratio of the isocyanate tripolymer to the blocking agent is 1.0-1.1: 1.
More preferably, the polyglutamic acid in the step 3) is a raw material of cosmetic grade, and the number/average molecular weight of the polyglutamic acid is 1000-1000000; the molar ratio of the isocyanate tripolymer to the polyglutamic acid is 2-3: 1.
Preferably, the finish is applied to the textile surface by a pad-bake process and the wash-resistant, moisture-retaining, soil-release and softness properties of the finished textile are achieved by deblocking of the blocked isocyanate and covalent crosslinking of the isocyanate and hydroxyl groups.
More preferably, the speed of the rolling and baking process is 30-80 m/min, and the baking temperature is 130-160 ℃. Can be adjusted according to the area density of the cotton fabric.
More preferably, the moisture regain of the finished textile is 9% -10%, and the soil release grade is 3-4.
The invention adopts two functional polymers, selects modified polyorganosiloxane with a specific structure to carry out reasonable compounding to carry out cotton fabric processing to obtain cotton textiles with target functions, and usually adopts processing equipment and process, namely, an open width tenter is adopted to carry out baking process to realize finishing processing of the textiles to obtain the cotton textiles with washing-resistant, moisture-retaining, soil-release and soft hand feeling characteristics.
The textile prepared by the invention is safe and environment-friendly, has excellent effect, can be used as underwear fabric and bed fabric, and has the functions of softness, moisture retention and easiness in washing; the functional finishing process is simple and easy to implement, the process is easy to control, and the large-scale production is facilitated.
Detailed Description
In order to make the invention more comprehensible, preferred embodiments are described in detail below.
The preparation method of the waterborne modified polyurethane structure finishing agent in the embodiment 1-2 comprises the following steps:
weighing 2000g of polyethylene glycol ether dihydric alcohol with the number average molecular weight of 2000, placing the polyethylene glycol ether dihydric alcohol in a vacuum reaction kettle at the temperature of 120 ℃ for dehydration for 8 hours, sampling, measuring the water content of the polyethylene glycol ether dihydric alcohol by using a Karl Fischer method, stopping dehydration when the water content is reduced to 0.02 percent, introducing nitrogen into the reaction kettle, and reducing the temperature to 75 ℃; weighing 1110.0g of HDI trimer, adding the HDI trimer into a reaction kettle, carrying out nitrogen protection reaction for 3 hours at 75 ℃, then adding 1.2g of organic tin, continuing catalytic reaction for 3 hours, using anhydrous acetone as a solvent, adding 31g of anhydrous ethylene glycol according to the weight ratio of 1: 1, continuing chain extension reaction for 3 hours, adding 182g of anhydrous butanone oxime as an end capping agent, continuing reaction for 2.5 hours at the same temperature, cooling to 60 ℃, adding 1500g of polyglutamic acid with the molecular weight of 1000 and 4823g of water solution, carrying out chain extension reaction for 5 hours, then cooling to 25 ℃, adjusting the pH value of the solution to be neutral by using sodium hydroxide, and obtaining a light yellow transparent aqueous solution with the solid content of 50%.
Example 1
Selecting cotton needle single jersey (160 g/m)2) The finishing agent is a waterborne modified polyurethane structure finishing agent and a waterborne polyether modified amino organic silicon structure finishing agent. The working solution is synthesized by 60g of waterborne modified polyurethane structure finishing agent, 30g of waterborne polyether modified amino organic silicon structure finishing agent, JFC 2g and the balance of water, and the total weight is 1000 g.
The finishing process flow comprises the following steps: padding the pure cotton knitted fabric, wherein the mangle ratio is 90%; baking at 130 deg.C for 3 min.
The standard moisture regain of the finished all-cotton textile is 9.6%, and the soil release grade is 3-4 (standard FZ-T0118-2012).
Example 2
Selecting cotton woven fabric (plain weave, 180 g/m)2) The finishing agent is a waterborne modified polyurethane structure finishing agent and a waterborne polyether modified amino organic silicon structure finishing agent. The working solution is synthesized by 80g of waterborne modified polyurethane structure finishing agent, 40g of waterborne polyether modified amino organic silicon structure finishing agent, 2.5g of JFC2 and the balance of water, and the total weight is 1000 g.
The finishing process flow comprises the following steps: padding the pure cotton knitted fabric, wherein the mangle ratio is 90%; baking at 150 deg.C for 2 min.
The standard moisture regain of the finished all-cotton textile is 9.5%, and the soil release grade is 3-4 (standard FZ-T0118-2012).
Example 3
Selecting cotton woven fabric (plain weave, 130 g/m)2) The finishing agent is a waterborne modified polyurethane structure finishing agent and a waterborne polyether modified amino organic silicon structure finishing agent. The working solution is synthesized by 60g of waterborne modified polyurethane structure finishing agent, 30g of waterborne polyether modified amino organic silicon structure finishing agent, 1.5g of JFC1 and the balance of water, and the total weight is 1000 g.
The finishing process flow comprises the following steps: padding the pure cotton knitted fabric, wherein the mangle ratio is 90%; baking at 150 deg.C for 2 min.
The standard moisture regain of the finished all-cotton textile is 9.0%, and the soil release grade is 3-4 (standard FZ-T0118-2012).

Claims (6)

1. A method for preparing soft all-cotton textile with washing resistance, moisture retention and easy decontamination is characterized in that two finishing agents are adopted to finish the all-cotton textile, wherein one finishing agent is waterborne modified polyurethane which comprises a polyglutamic acid chain segment and a polyether chain segment and contains reactive blocked isocyanate; the other is water-based polyether modified amino organic silicon which contains segmented amino siloxane chain links and polyether chain link structures;
the preparation method of the waterborne modified polyurethane comprises the following steps:
step 1): reacting isocyanate tripolymer and dehydrated high-molecular dihydric alcohol in a reaction kettle at 50-95 ℃ for 2-6 h under the action of a catalyst; the isocyanate tripolymer adopts an aliphatic isocyanate tripolymer or an aromatic toluene diisocyanate tripolymer; the number average molecular weight of the dehydrated macromolecule dihydric alcohol is 500-15000; the molar ratio of the isocyanate tripolymer to the dehydrated high-molecular diol is 2.1-2.4: 1;
step 2): adding micromolecular dihydric alcohol into a reaction kettle to perform chain extension reaction for 2-3 h, and then adding an end capping agent to continue the reaction for 2-3 h; the micromolecular dihydric alcohol adopts ethylene glycol, propylene glycol, butanediol or 1, 4-dihydroxymethylbenzene; the end-capping reagent adopts oxime compounds; the mole ratio of the dehydrated macromolecule dihydric alcohol to the micromolecule dihydric alcohol is 4.1-4.2: 1; the molar ratio of the isocyanate trimer to the blocking agent is 1.0-1.1: 1;
step 3): cooling the reaction kettle to 50-60 ℃, adding a polyglutamic acid aqueous solution with the pH value of 4-5, and carrying out chain extension reaction for 4-6 h; the polyglutamic acid is a cosmetic raw material, and the number average molecular weight of the polyglutamic acid is 1000-1000000; the molar ratio of the isocyanate tripolymer to the polyglutamic acid is 2-3: 1;
step 4): cooling the reaction kettle to 25 ℃, and adjusting the pH value to be neutral by using sodium hydroxide;
the dehydrated high-molecular dihydric alcohol in the step 1) adopts polyoxyethylene ether dihydric alcohol, block dihydric alcohol of polyoxyethylene polyoxypropylene ether or mixture of two types of dihydric alcohol.
2. The method for preparing the washing-resistant, moisturizing and soil-releasing soft all-cotton textile according to claim 1, wherein the number average molecular weight of the polyglutamic acid chain segment is not less than 1000, and the weight percentage of the molecular chain segment in the waterborne modified polyurethane structure is more than 25%; the weight percentage of the polyether chain segment in the waterborne modified polyurethane structure is more than 50 percent.
3. The method for preparing the soft all-cotton textile with washing resistance, moisture retention and soil release according to claim 1, wherein the amino organosilicon is a polymethyl siloxane macromolecular chain, and the side group of the polymethyl siloxane macromolecular chain contains aminopropyl, N- (beta-aminoethyl) -gamma-aminopropyl or gamma- (2, 3-epoxy propoxy) propyl reactive group; the polyether chain structure is a polyepoxy ethyl ether structure or a block ether structure of epoxy ethylene and epoxy propylene.
4. A process for the preparation of a wash durable, moisture retaining, soil release soft all cotton textile according to claim 1 wherein the finish is applied to the textile surface by a pad bake process and the wash durable, moisture retaining, soil release and soft properties of the finished textile are achieved by deblocking of the blocked isocyanate and covalent crosslinking of the isocyanate and hydroxyl groups.
5. The method for preparing the washing-resistant, moisturizing and soil-releasing soft all-cotton textile according to claim 4, wherein the rolling and baking process is carried out at a speed of 30-80 m/min and a baking temperature of 130-160 ℃.
6. The method for preparing the washing-resistant, moisturizing and soil-release soft all-cotton textile according to claim 4, wherein the moisture regain of the finished textile is 9% -10%, and the soil release grade is 3-4.
CN201810396357.4A 2018-04-27 2018-04-27 Preparation method of washing-resistant, moisturizing, easy-decontamination and soft cotton textiles Expired - Fee Related CN108547152B (en)

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CN111205428B (en) * 2018-11-22 2022-03-08 香港理工大学深圳研究院 Polyurethane-urea fiber material and preparation method and application thereof
CN112778498B (en) * 2019-11-05 2023-05-26 万华化学集团股份有限公司 Aqueous modified polyurethane dispersoid and application thereof and hair conditioner prepared from aqueous modified polyurethane dispersoid
CN112921662A (en) * 2021-02-02 2021-06-08 鲁泰纺织股份有限公司 Finishing process of pure cotton non-ironing soil-release fabric

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